# Intraoperative hypotension after remimazolam or propofol induction with sevoflurane maintenance in angiotensin II receptor blockers-treated patients: a randomized controlled trial

**Authors:** Hye Jin Kim, Namo Kim, Jiho Kim, Jin Ha Park, Hye Jung Shin, Jinho Yang, So Yeon Kim

PMC · DOI: 10.1038/s41598-025-23469-y · 2025-11-13

## TL;DR

This study compared remimazolam and propofol for reducing hypotension during prostate surgery in patients on blood pressure drugs, finding no significant difference between the two.

## Contribution

The study is the first to compare remimazolam and propofol for intraoperative hypotension in ARB-treated patients undergoing RALP.

## Key findings

- No significant difference in hypotension incidence between remimazolam and propofol groups.
- No significant differences in secondary endpoints like MAP thresholds or norepinephrine use.
- Remimazolam did not reduce hypotension risk compared to low-dose propofol in ARB-treated patients.

## Abstract

Robot-assisted laparoscopic prostatectomy (RALP) is associated with hemodynamic shifts; patients on angiotensin receptor blockers (ARBs) are especially susceptible to intraoperative hypotension. We investigated whether induction with remimazolam reduces the intraoperative hypotension incidence and severity compared with propofol in this population. Herein, 112 hypertensive patients undergoing RALP who continued ARB therapy received remimazolam (0.2 mg/kg) or propofol (1–1.5 mg/kg) for anesthetic induction. The primary endpoint was hypotension occurrence (mean arterial pressure [MAP] < 65 mmHg sustained for ≥ 1 min), assessed during the entire anesthesia and 15 min post-induction. Secondary endpoints included MAP < 55 mmHg sustained for ≥ 1 min, time-weighted average (TWA)-MAP < 65 mmHg or < 55 mmHg, duration of MAP < 65 mmHg, and required norepinephrine dose. The hypotension incidence did not differ significantly between groups during the entire anesthesia (87.5% vs. 89.3%, P > 0.999). During the entire anesthesia, no significant between-group differences were observed for MAP < 55 mmHg for ≥ 1 min, TWA-MAP < 65 mmHg or < 55 mmHg, duration of MAP < 65 mmHg, and required norepinephrine dose. Similarly, no significant between-group differences were observed during the 15 min after induction. Induction with remimazolam did not reduce intraoperative hypotension risk compared with low-dose propofol in patients undergoing RALP who continued ARB therapy.

Clinical trial registration number: ClinicalTrials.gov (NCT06093971, 23/10/2023).

## Linked entities

- **Chemicals:** remimazolam (PubChem CID 9867812), propofol (PubChem CID 4943), norepinephrine (PubChem CID 951)

## Full-text entities

- **Diseases:** hypertensive (MESH:D006973), hypotension (MESH:D007022)
- **Chemicals:** propofol (MESH:D015742), remimazolam (MESH:C522201), norepinephrine (MESH:D009638), sevoflurane (MESH:D000077149)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12615582/full.md

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Source: https://tomesphere.com/paper/PMC12615582